7q36

A chromosome band present on 7q
National Institutes of Health

Topic mentions per year

Topic mentions per year

1986-2017
05101519862017

Papers overview

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Highly Cited
2009
Highly Cited
2009
Idiopathic Ventricular Fibrillation (IVF) is defined as spontaneous VF without any known structural or electrical heart disease… (More)
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Highly Cited
2003
Highly Cited
2003
Unequivocal identification of the full composition of a gene is made difficult by the cryptic nature of regulatory elements… (More)
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Highly Cited
2003
Highly Cited
2003
PURPOSE To map the gene(s) associated with autosomal dominant (AD) high-grade myopia. METHODS A multigeneration English… (More)
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Highly Cited
2002
Highly Cited
2002
High myopia often appears as a familial disease. It is usually defined as a refraction error equal to or below −6 diopters (D) in… (More)
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1999
1999
Pre-eclampsia is the most common serious medical disorder of human pregnancy. The human endothelial cell nitric oxide synthase… (More)
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1997
1997
Holoprosencephaly (HPE) is a genetically heterogeneous disorder that affects the midline development of the forebrain and midface… (More)
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Highly Cited
1996
Highly Cited
1996
Holoprosencephaly (HPE) is a common developmental defect of the forebrain and frequently the midface in humans, with both genetic… (More)
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1995
1995
Sacral agenesis is a rare disorder of uncertain incidence1 that has been reported in diverse populations. Although usually… (More)
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1994
1994
We demonstrate that the gene responsible for a congenital limb deformity (polysyndactyly) maps to chromosome 7q36 in a large… (More)
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1993
1993
Holoprosencephaly (HPE) is a developmental field defect involving the brain and face. Cytogenetic deletions in patients with HPE… (More)
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